Supercapacitor energy storage devices are well suited to meet the rigorous demands of future portable consumer electronics (PCEs) due to their high energy and power densities (i.e., longer battery-life and rapid charging, respectively) and superior operational lifetimes (10 times greater than lithium-ion batteries). To date, research efforts have been narrowly focused on improving the specific capacitance of these materials; however, emerging technologies are increasingly demanding competitive performance with regards to other criteria, including scalability of fabrication and electrochemical stability. In this regard, we developed a polyaniline (PANI) derivative that contains a carbazole unit copolymerized with 2,5-dimethyl-p-phenylenediamine (Cbz-PANI-1) and determined its optoelectronic properties, electrical conductivity, processability, and electrochemical stability. Importantly, the polymer exhibits good solubility in various solvents, which enables the use of scalable spray-coating and drop-casting methods to fabricate electrodes. Cbz-PANI-1 was used to fabricate electrodes for supercapacitor devices that exhibits a maximum areal capacitance of 64.8 mF cm–2 and specific capacitance of 319 F g–1 at a current density of 0.2 mA cm–2. Moreover, the electrode demonstrates excellent cyclic stability (≈ 83% of capacitance retention) over 1000 CV cycles. Additionally, we demonstrate the charge storage performance of Cbz-PANI-1 in a symmetrical supercapacitor device, which also exhibits excellent cyclic stabilitymore »
One-step hydrothermal synthesis of porous Ti 3 C 2 T z MXene/rGO gels for supercapacitor applications
Titanium carbide/reduced graphene oxide (Ti 3 C 2 T z /rGO) gels were prepared by a one-step hydrothermal process. The gels show a highly porous structure with a surface area of ∼224 m 2 g −1 and average pore diameter of ∼3.6 nm. The content of GO and Ti 3 C 2 T z nanosheets in the reaction precursor was varied to yield different microstructures. The supercapacitor performance of Ti 3 C 2 T z /rGO gels varied significantly with composition. Specific capacitance initially increased with increasing Ti 3 C 2 T z content, but at high Ti 3 C 2 T z content gels cannot be formed. Also, the retention of capacitance decreased with increasing Ti 3 C 2 T z content. Ti 3 C 2 T z /rGO gel electrodes exhibit enhanced supercapacitor properties with high potential window (1.5 V) and large specific capacitance (920 F g −1 ) in comparison to pure rGO and Ti 3 C 2 T z . The synergistic effect of EDLC from rGO and redox capacitance from Ti 3 C 2 T z was the reason for the enhanced supercapacitor performance. A symmetric two-electrode supercapacitor cell was constructed with Ti 3 C more »
- Award ID(s):
- 1760859
- Publication Date:
- NSF-PAR ID:
- 10322062
- Journal Name:
- Nanoscale
- Volume:
- 13
- Issue:
- 39
- ISSN:
- 2040-3364
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract 2D material hydrogels have recently sparked tremendous interest owing to their potential in diverse applications. However, research on the emerging 2D MXene hydrogels is still in its infancy. Herein, we show a universal 4D printing technology for manufacturing MXene hydrogels with customizable geometries, which suits a family of MXenes such as Nb 2 CT x , Ti 3 C 2 T x , and Mo 2 Ti 2 C 3 T x . The obtained MXene hydrogels offer 3D porous architectures, large specific surface areas, high electrical conductivities, and satisfying mechanical properties. Consequently, ultrahigh capacitance (3.32 F cm −2 (10 mV s −1 ) and 233 F g −1 (10 V s −1 )) and mass loading/thickness-independent rate capabilities are achieved. The further 4D-printed Ti 3 C 2 T x hydrogel micro-supercapacitors showcase great low-temperature tolerance (down to –20 °C) and deliver high energy and power densities up to 93 μWh cm −2 and 7 mW cm −2 , respectively, surpassing most state-of-the-art devices. This work brings new insights into MXene hydrogel manufacturing and expands the range of their potential applications.
-
Micro-supercapacitor is a member of the miniaturized energy storage device family, which offers great advantages on power density and life span. However, the limited device capacitance and narrow voltage window limit its energy density, hindering its application. In the present work, a novel micro-pseudocapacitor (MPC) constructed via the facile extrusion-based 3D printing technique has been demonstrated to deliver efficient charge storage with high device capacitance and moderate voltage window. Such an asymmetric MPC is constructed with 3D-printing-enabled asymmetric interdigitated cellular microelectrodes; in which, one is Ni–Co–O nanosheets grown on macroporous 3D reduced GO (3DG) microelectrode and the other is MnO 2 nanosheets grown on 3DG. Such an MPC offers facilitated fast electron transport, ionic diffusion, large number of active sites and desired porosity for electrolyte penetration. The asymmetric MPC shows a high specific capacity of 500 mC cm −2 , an energy density of 90 μW h cm −2 and a voltage window of 1.3 V. A device cycling stability with 10 000 charge and discharge cycles is also achieved for the as-fabricated asymmetric MPCs. These encouraging results may open a new avenue to design and fabricate state-of-the-art miniaturized electrochemical energy storage devices with customized geometries.
-
Recently, graphene fibers derived from wet-spinning of graphene oxide (GO) dispersions have emerged as viable electrodes for fiber-shaped supercapacitors (FSCs) and/or batteries, wherein large surface area, high electrical conductivity, and sufficient mechanical strength/toughness are desired. However, for most fiber electrodes reported so far, compromises have to be made between energy-storage capacity and mechanical/electrical performance, whereas a graphene fiber with high capacity and sufficient toughness for direct machine weaving or knitting is yet to be developed. Inspired by the alum mordant used for natural dyes in the traditional textile dyeing industry, our research group has synthesized wet-spun GO fibers and coagulated them with different multivalent cations ( e.g. Ca 2+ , Fe 3+ , and Al 3+ ), where dramatically different fiber morphologies and properties have been observed. The first principles density functional theory has been further employed to explain the observed disparities via cation–GO binding energy calculation. When assembled into solid-state FSCs, Al 3+ -based reduced GO (rGO) fibers offer excellent stability against bending, and a specific capacitance of 148.5 mF cm −2 at 40 mV s −1 , 1.4, 4.8, and 6.8 times higher than that of the rGO fibers based on other three coagulation systems (Fe 3+ ,more »
-
Advances in the synthesis and processing of graphene-based materials have presented the opportunity to design novel lithium-ion battery (LIB) anode materials that can meet the power requirements of next-generation power devices. In this work, a poly(methacrylic acid) (PMAA)-induced self-assembly process was used to design super-mesoporous Fe 3 O 4 and reduced-graphene-oxide (Fe 3 O 4 @RGO) anode materials. We demonstrate the relationship between the media pH and Fe 3 O 4 @RGO nanostructure, in terms of dispersion state of PMAA-stabilized Fe 3 O 4 @GO sheets at different surrounding pH values, and porosity of the resulted Fe 3 O 4 @RGO anode. The anode shows a high surface area of 338.8 m 2 g −1 with a large amount of 10–40 nm mesopores, which facilitates the kinetics of Li-ions and electrons, and improves electrode durability. As a result, Fe 3 O 4 @RGO delivers high specific-charge capacities of 740 mA h g −1 to 200 mA h g −1 at various current densities of 0.5 A g −1 to 10 A g −1 , and an excellent capacity-retention capability even after long-term charge–discharge cycles. The PMAA-induced assembly method addresses the issue of poor dispersion of Fe 3 O 4 -coatedmore »